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Sample GSM4196310 Query DataSets for GSM4196310
Status Public on Nov 30, 2019
Title scRNA-seq [N709-N517]
Sample type SRA
 
Source name colon tumor cells
Organism Mus musculus
Characteristics strain: ApcMin/+
age: 12 weeks
Sex: male
tissue: colon
cell type: DAPI-Cd31-Cd45-Epcam+Cd24+ cells
Treatment protocol Male ApcMin/+ mice between 10 weeks of age were given 2% (w/v) Dextran sulfate sodium salt (DSS) (MP Biomedicals, #0216011090) in drinking water for 5 days
Extracted molecule polyA RNA
Extraction protocol DAPI-Cd31-Cd45-Epcam+Cd24+ cells were single-cell sorted.
FACS-sorted single cells were subjected to cDNA synthesis using Bead-seq method (DOI:10.1016/j.ab.2014.10.011, DOI:10.1038/s41598-017-04616-6). The processes from the production of cDNA libraries to their amplification and first purification were carried out automatically using a Caliper Zephyr compact liquid handler (Perkin Elmer, CA, USA).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description 160120_Hiseq3B_l8_009_Dr_Okamoto_N709-N517_GCTACGCT-GCGTAAGA_L008
Data processing Basecalling was performed using configureBclToFastq.pl of bcl2fastq version 1.8.4 with the following arguments: --with-failed-reads --no-eamss --use-bases-mask Y*,I8,I8
Reference sequences for mapping were prepared using rsem-prepare-reference of RSEM version 1.2.31 and Bowtie2 version 2.2.9.
Reads were filtered and trimmed using prinseq-lite.pl of PRINSEQ version 0.20.4 with the following arguments: -min_len 30 -trim_tail_right 5 -trim_tail_left 5 -min_qual_mean 20 -trim_qual_right 20 -trim_qual_left 20
The processed reads were mapped to the reference sequences and TPM (Transcripts Per Million) were calculated using rsem-calculate-expression of RSEM version 1.2.31 and Bowtie2 version 2.2.9 with the default parameters.
Gene TPM values were extracted from TPM columns of RSEM gene result files.
Genome_build: GRCm38.p4
Supplementary_files_format_and_content: CSV file including TPM values; The column labels are single cell names, and the row labels are gene IDs.
 
Submission date Nov 29, 2019
Last update date Dec 01, 2019
Contact name Daichi Narushima
Organization name National Cancer Center Research Institute
Department Department of Bioinformatics
Street address 5-1-1 Tsukiji, Chuo-ku
City Tokyo
ZIP/Postal code 104-0045
Country Japan
 
Platform ID GPL17021
Series (1)
GSE141157 PROX1 mediates chemoresistance-associated recurrence via maintenance of quiescent colon cancer stem cells
Relations
BioSample SAMN13427388
SRA SRX7241530

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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